Abstract: A body fluid testing device includes a test strip, an incision forming member, and a housing. The test strip includes an expression surface. In addition, the test strip is attached to the housing to form a cavity, and the cavity slidably receives the incision forming member. The body fluid testing device is positioned over the incision site where the incision forming member makes an incision. The user presses the expression surface against the skin to express body fluid. The cavity collects body fluid via capillary action, and the test strip analyzes the body fluid.

Abstract: A puncturing device for generating a puncture wound to sample a body fluid is provided and comprises a press-on part or contact element to be pressed against a body part to generate a puncture, a test sensor for measuring a test parameter value, and an analytical unit for determining whether the value of the measured test parameter satisfies a predefined minimum requirement for successful sampling. In one embodiment, the value of the test parameter is monitored during a waiting period by the test sensor once the value satisfies the predefined minimum requirement. After the waiting period has elapsed, so long as the values of the test parameter monitored during the waiting period are in a range of values that predicts sampling to be successful, the analytical unit initiates a puncture.

Abstract: Body fluid sampling device comprising a skin-piercing element having a collection zone for receiving body fluid, the device further comprising a fluid receiving means remotely spaced apart from the collection zone so that body fluid in the collection zone will not contact the fluid receiving means initially. The collection zone takes up a very small volume of body fluid of about 10 to 500 nl in a very short time period of less than 0.5 seconds. The fluid receiving means may have a test zone for performing an analytical reaction. Fluid sample from the collection zone is automatically or manually transported to the fluid receiving means to contact the fluid with the test zone.

Abstract: Systems for and methods of assessing lower urinary tract function from urinary flow data via sound analysis and user-provided information regarding the lower urinary tract symptoms (LUTS) of frequency, urgency and urge incontinence. Embodiments of the LUTS assessment systems include a computer and a telephone or a digital recording mechanism to capture the sound of one or more urination events, which are stored as audio files in a database. The LUTS assessment systems may include sound analysis software for analyzing the strength and duration of each urination event and may include a web-based software application for viewing the results via the Internet or other network. The database stores information from multiple urination events, and combined with information regarding the lower urinary tract symptoms, serves as an objective tool to assess bladder function and monitor progression of disease or therapy effectiveness.

Abstract: A closed blood sampling system within a pressure monitoring line having a control valve that enables a clearance reservoir to be isolated from the pressure column when no samples are being taken. The valve is a stopcock-like device that includes a rotating valve member and attached control handle with clear visible and tactile indicators for the mode of operation. The rotating valve member has a number of internal and circumferential channels for connecting or disconnecting select ports in the core of the valve. By isolating the clearance reservoir, the quality of the pressure signal is improved such that the sampling line can be lengthened for greater convenience in the intensive care or operating room. The valve may also incorporate a blunt cannula sampling site therewithin.

Abstract: An integrated patient monitoring and control system is provided which includes a SITS, the SITS being adapted for coupling to the patient to obtain a specimen from the patient, a sensor, the sensor being adapted to receive the specimen from the SITS and to analyze the sample, a medication control unit, the medication control unit receiving information from the sensor, and utilizing that information to determine medication dosing information for the patient, and a medication administration system, the medication administration system receiving the dosing information from the medication control unit, and adapted to cause administration of the medication to the patient. If the SITS is adapted for blood draw, the system advantageously is performed in conjunction with a pneumatic pressure cuff, inflated so as to aid in blood draw.

Abstract: A sampling device for sampling body fluid includes a lancet for making an incision, a capillary tube for drawing-up body fluid from the incision, and a test strip affixed to an upper end of the capillary tube for receiving the fluid. An absorbent pad can be disposed between the test strip and capillary tube for spreading-out the fluid being transferred to the test strip. An on-site analyzer such as an optical analyzer and/or an electrochemical analyzer can be mounted in the device for analyzing the fluid. Alternatively, a test strip can be slid through a slot formed in the bottom end of the device so that by passing the device against the skin after an incision has been formed, the test strip will directly contact body fluid emanating from the incision.

Abstract: The present invention concerns a body fluid testing device (10) for analyzing a body fluids, comprising a test media tape (30) adapted to collect the body fluid, a supply portion (100) storing an uncontaminated section of the test media tape, a storage portion (110) for storing a contaminated section of the test media tape, an exposure portion positioned between the supply portion and the storage portion, the exposure portion being adapted to expose a section of the test media tape to the body fluid. An important aspect is a tip portion (20) for exposing a test medium to body fluid application. The application further concerns a test media cassette for housing test media. Another aspect is a testing device and method that employs illumination of a test medium at the site for body fluid application.

Abstract: Multi-functional urine collection devices, embodiments of which can include a self-expanding container having a receptacle for receiving urine from the tubing, a pump for moving urine through the tubing and into a receptacle, extendable tubing that may be shortened and/or lengthened, and/or one or more meters for monitoring, measuring, transmitting or storing a characteristic from the urine. The urine collection system may include a widened profile to permit urine to cascade from one column to the another and/or may include one or more floats to minimize meniscus errors. The floats may include active agents, may change color based on pH, and may be calibrated to indicate the specific gravity of the urine.

Abstract: A method and system for determining the residual volume within a patient having a naso-enteral feeding tube. A collection container is coupled to the naso-enteral feeding tube and a physical force is applied to the collection container to prevent stomach fluid from flowing into the collection container. The physical force is removed from the collection container and the stomach fluid is allowed to flow into the collection container. The volume of fluid within the collection container is determined, which represents the gastric residual volume of the patient. At least a portion of the collected volume of stomach fluid is returned to the patient from the collection container.

Abstract: A sampling device for sampling body fluid includes a lancet for making an incision, a capillary tube for drawing-up body fluid from the incision, and a test strip affixed to an upper end of the capillary tube for receiving the fluid. An absorbent pad can be disposed between the test strip and capillary tube for spreading-out the fluid being transferred to the test strip. An on-site analyzer such as an optical analyzer and/or an electrochemical analyzer can be mounted in the device for analyzing the fluid. Alternatively, a test strip can be slid through a slot formed in the bottom end of the device so that by passing the device against the skin after an incision has been formed, the test strip will directly contact body fluid emanating from the incision.

Abstract: A blood glucose measuring system includes a lancet assembly and a meter for use with the lancet assembly. The lancet assembly has a lancet member with a lance, a lancet body having a drive wing extending outwardly from a side, and a sinuous portion, and an elongated carrier having a lancet member recess to contain the lancet member. The elongated carrier has an open end, a closed end, a side elongated opening for receiving the drive wing therethrough, and an anchoring member operatively connected to the end of the sinuous portion. The meter includes a measuring circuit, a lancet trigger, and a lancet driver where the lancet driver includes a driver piston engageable with the lancet trigger and a charging member that operatively engages with the driver piston to move the driver piston into an armed position and to stop the driver piston when released from the armed position.

Abstract: A lancet assembly has a lancet body with a needle end, a sinuous portion end, and a slot, a lancet tip connected to the needle end, a sinuous portion connected to the sinuous portion end, an anchor structure connected to the sinuous portion. The lancet assembly may also include a lancet enclosure having an elongated chamber with a needle end, an anchor end in communication with the elongated chamber opposite the needle end, and a lancet enclosure slot in communication with the elongated chamber and spaced from the needle end. The anchor end is configured to receive and hold the anchor structure in a substantially static position. The elongated chamber is sized to receive in sliding engagement the lancet tip, the lancet body where the lancet body slot is in communication with the lancet enclosure slot and the sinuous portion and to permit slidable movement of the lancet tip through the open end between a retracted position and an extended position.

Abstract: An improved system for mammography analysis and methods of using the same. In one aspect, a clip comprises a first portion and at least one additional second portion connected to the first portion, the first and second portions adapted for elastic deformation for engaging tissue. In anther aspect, an improved actuator for performing a breast biopsy is used to deploy a clip. In yet another aspect of the invention, there is contemplated a system for marking an evacuated breast cyst.

Abstract: A continuous Glomerular Filtration Rate (GFR) estimation system may include a Foley catheter, a continuous urine creatinine sensor, and a urine output monitor. The continuous GFR estimation system computes creatinine clearance as CrCl=(Ucr×Uvol)/(Pcr×Imim), where Ucr is urine creatinine in mg/dL, Uvol is urine volume in mL, Pcr is plasma (serum) creatinine in mL, and Imin is time in minutes. A Foley catheter may be used to withdraw urine from the bladder. The urine may be delivered to a urine output monitor that provides the Uvol value over a time Imin. Attached to the catheter is the flow-through continuous urine creatinine sensor for providing the Ucr value. The remaining parameter is Pcr. Because serum creatinine levels do not change rapidly over time, a blood sample may be withdrawn prior to the start of the continuous GFR to obtain the PCr value.

Abstract: A method and device for processing mammalian adipose tissue such that the vascular rich fraction is separated from the vascular poor fraction, Mammalian adipose tissue in the form of morselated surgical biopsies and/or lipoaspirate from liposuction is placed within a novel syringe attached to a detection device measuring either color, light saturation, infra-red light, heme, iron or oxygen saturation. This process involves no label and minimal manipulation and handling of the tissue. This process and device may also be used intra-operatively under sterile conditions for immediate use within the same individual receiving liposuction or surgery.

Abstract: A lancet integrated test element (LIT) includes an incision forming member that has a cutting end configured to form an incision in tissue. A test element is attached to the incision forming member to test fluid from the incision. The test element has a sampling end with a sample opening through which the fluid is collected. The test element is bendable from a first state where the cutting end of the incision forming member is retracted from the sampling end of the test element to a second state where at least a portion of the cutting extends past the sampling end of the test element to form the incision in the tissue.

Abstract: A meter system for analyzing body fluids includes a supply magazine for storing a stack of test elements, a meter for analyzing fluid samples, and a transport system for transporting test elements from the supply magazine to the meter. The test element in one embodiment includes a lancet integrated test element that has a lancet coupled to a test strip. The transport system is configured to minimize damage to the test element. In one form, the transport system includes a shuttle that slides the top-most test element from the stack onto a connection portion of the meter. In another form, the transport system includes a drum that rotates to transport test elements from the supply magazine to a testing position and, once used, to a waste magazine for disposal. In a further form, the transport system includes a disc that rotates to transport the test elements.

Abstract: An apparatus and method for the detection of substances in an excretion. A diaper is generally utilized and a pad containing one or more reagent strips is placed within a sleeve in the crotch of the diaper. An excretion within the diaper, such as urine, occurs and the reagent strips are activated and test for the presence of certain substances. The substances tested for are generally ones in which mothers may abuse and are harmful to and transferred to the infant, but may be any substance the presence of such is helpful to know.

Abstract: Described is, e.g., an apparatus (100), and associated methods of manufacture and use, for draining a fluid, discharged from a urinary catheter (104) installed in a subject's bladder, into a drain container (138) while avoiding undesired pressure states in such bladder. A drain conduit (102) connected to the catheter has a sufficiently small size as to maintain plug-flow between opposite ends of the drain conduit. The discharge end of the drain conduit is connected to a siphon-break apparatus (106) configured to cause a siphon-break disposed at an elevation (132) in approximate agreement with the subject's bladder. The potential energy from fluid downstream of the siphon-break location is decoupled from fluid in the drain conduit.

Abstract: Devices and methods for positioning a portion of a sensor at a first predetermined location, displacing the portion of the sensor from the first predetermined location to a second predetermined location, and detecting one or signals associated with an analyte level of a patient at the second predetermined location are disclosed. Also provided are systems and kits for use in analyte monitoring.

Abstract: The invention relates to a medical aid which comprises a lancet (2) with a proximal end (5) and a distal end, the lancet (2) having a lancet body (4) and, at the proximal end (5), a lancet tip (3). The lancet (2) is at least partially enclosed by a packaging that comprises at least one flexible film section (7, 8) having a distal end (12), a proximal end (16), a first lateral edge and a second lateral edge. The lancet (2), at least partially enclosed by the packaging, is arranged displaceably between an upper protective section (9) and a lower protective section (10). The at least one flexible film section (7, 8) is detachably connected, along at least one segment of its first and second lateral edges, to an additional flexible film section (7, 8) or to one of the protective sections (9, 10).

Abstract: An integrated sampling device defines a first opening and a second opening. The first opening is connected to a channel for drawing fluid automatically towards a test media upon incision by an incision portion. The second opening is positioned over the test media allowing manual sampling of fluid if the channel fails to draw a sufficient amount of fluid onto the test media.

Abstract: An apparatus for lancing skin and collecting a liquid sample. The apparatus having a housing with an outer periphery and a rotatable arm having a lance to puncture the skin. A sample collection area is attached to the arm. The arm of the apparatus rotates from a first position to a second position. As the arm rotates, the lance extends beyond the housing allowing the lance to contact the user's skin and create a lance site. As the arm continues to move to the second position, the lance is brought out of contact with the user's skin and back within the housing while the collection area is brought into position. When the arm is located in the second position, the collection area is in substantially the same location as the lance site on the user's skin.

Abstract: Apparatus for quick screening for vaginal moisture pH level and for amine associated with such moisture, comprising a manipulable element including a probe insertable into the vagina; a pH indicator on a first side of the element, the indicator characterized as producing a color which corresponds to pH level of vaginal moisture contacting the indicator; and a second indicator on a second side of the element, the second indicator elongated lengthwise of the element and being an amine indicator, the second indicator having an outer surface exposed to vaginal moisture, the surface presenting a sequence of crests for collection of moisture between crests in response to movement of the element in the vagina.

Abstract: A cassette containing cartridges for sampling blood from a patient. The cassette includes a container for storing a plurality of cartridges and at least one cartridge in the container. The cartridge includes a cartridge case and a lancet. The lancet has a tip and is housed in the cartridge case. The lancet can be driven to extend the tip outside the cartridge case for lancing the skin of the patient to yield blood. The container has a compartment that contains at least one cartridge. A cartridge from the compartment can be loaded onto a glucometer that drives the lancet in the cartridge to lance the skin of a patient.

Abstract: A urine collection system includes an anti-flux mechanism to reduce the amount of urine that may flow from within the collection bag back into the urine meter. The urine collection system includes a urine meter, a collection member defining at least a first opening for receiving urine from the urine meter and a shield positioned adjacent the opening of the collection member. The shield is affixed to the collection member at predetermined connection points along a periphery of the shield whereby urine flows between the connection points from the urine meter to the collection member. The shield may be affixed to an internal surface of the bag. The shield may be spot welded to the collection member at the connection points. The shield may include at least a first slot configured to permit the passage of fluid therethrough.

Abstract: A bodily fluid sampling device is operable to breach the skin surface and allow bodily fluid to emerge from the breach location. The bodily fluid sampling device further evaluates the amount of bodily fluid emerged from breach location and determines whether the amount is sufficient or insufficient for a particular purpose, such as sampling and testing. The determination is accomplished automatically without moving the device. The user may also intervene to perform a variety of tasks following the determination of the amount of bodily fluid.

Abstract: A urological instrument (1) for assessing a urine flow, includes a receiving member (5) for the urine flow which, at least during operation, is in open liquid communication with a urine guide (6). The urine guide (6) leads to an inlet of flow indicator element (7) for assessing at least a magnitude of the urine flow. The receiving member (5) has a first, relatively compact storage state and a second, expanded ready-to-use state and is designed and adapted to allow it to be brought manually from the storage state to the ready-to-use state. At least in the ready-to-use state the receiving member comprises a cavity open on at least one side for receiving the urine flow therein.

Abstract: These and other objects of the present invention are achieved in a body fluid sampling system for use on a tissue site that includes an electrically powered drive force generator. A penetrating member is operatively coupled to the force generator. The force generator moves the member along a path out of a housing having a penetrating member exit, into the tissue site, stops in the tissue site, and withdraws out of the tissue site. An analyte detecting member is positioned to receive fluid from a wound created by the penetrating member. The detection member is configured to determine a concentration of an analyte in the fluid using a sample of less than 1 ?L of the fluid.

Abstract: Monitoring the status of an absorbent article can be desirable to various users in various situations. A monitoring device for use with an absorbent article is provided. The monitoring device includes a sensing device and a signaling device. The sensing device is configured to sense a physiological indication related to the absorbent article wearer. The functionality of the monitoring device may be updateable, for instance, by utilizing firmware updates, hardware or user interface changes, software installations, etc. Thus, the monitoring device of the present invention may be utilized over an entire lifespan from infants to elderly without the need for costly replacement or installation of an entirely new monitoring system.

Abstract: There is provided a biosensor chip where the collecting amount necessary for the measurement is made small whereby burden of a user is reduced and, at the same time, a sample at a puncture opening is able to be easily collected and measured without an operation of making the sample collection opening nearer the puncture opening. When an end of a main body chip is pushed onto a test body, an elastic body installed at an end of the main body chip is compressed and a device for puncture is produced whereby the test body is able to be punctured. When the pushing force is made weak, the device for puncture is pulled out from the test body due to resilience of the elastic body and a sample is flown out from the puncture opening.

Abstract: The invention relates to a piercing device for creating a puncture wound for collecting a sample of body fluid, comprising a rubber elastic pressure part to be pressed onto a body part from which a sample of body fluid is to be removed, and a piercing drive mechanism by means of which a piercing element inserted into the piercing device can be driven in a piercing movement. According to the invention, an electrical deformation sensor is provided for detecting an elastic deformation of the pressure part by means of an electrical and/or magnetic measurement.

Abstract: A point of care fluid testing system for determining properties of a fluid comprises a patient connection, a primary fluid routing portion, a pump, a secondary fluid routing portion, and a flushing fluid connection. The patient connection connects the system to a patient. The primary fluid routing portion has a pump region, a fluid transfer region, and an in-line testing region. The pump region pumps the fluid sample from the patient to the testing portion and back to the patient. The in-line testing region evaluates a first characteristic of the fluid sample. The fluid transfer region transmits a portion of the fluid sample out of the primary fluid routing portion. The secondary fluid routing portion includes an off-line testing portion that receives the portion of the fluid sample transmitted from the fluid transfer region. The off-line testing portion evaluates a second characteristic of the fluid sample.

Abstract: Body fluid testing device for analyzing a body fluid comprises a test media tape adapted to collect the body fluid. The test media tape comprises a tape and test media portions. A free tape portion without test medium is located between successive test media portions. The testing device further comprises a supply portion. The supply portion comprises a housing in which uncontaminated test media tape is contained. The housing further has an opening for withdrawing test media tape from the housing. The testing device further has a sealing means for closing the opening against the surrounding. A free tape portion of the test media tape is located between a wall of the housing and the sealing means when the sealing means closes the opening. Further aspects concern a test media cassette with sealing means and a method for providing test media while holding them sealed against humidity during onboard storage.

Abstract: The invention relates to a system for collecting samples and to a method for collecting a liquid sample. The system comprises at least one analytical aid, the analytical aid comprising a lancet and a test element, and the test element having a test field for analysis of the liquid sample. The system for collecting samples comprises a coupling element which can be successively connected to the lancet, in a first position of the analytical aid, and to the test element, in a second position of the analytical aid. The system for collecting samples also comprises a drive unit for moving the coupling element from a rest position to a deployed position, such that the movement of the coupling element is transmitted to the lancet, coupled thereto, in order to execute a puncturing movement, or is transmitted to the test element, coupled thereto, in order to execute a sample recovery movement.

Abstract: A plurality of Point-of-Care (POC) tests on a single cartridge (300) is provided such that sequential or nonsequential tests may be performed in an integrated fashion without changing the test cartridge. Each cartridge can contain a penetrating member sensor (302) combination in a radial disk format, interrogated and read by a single illumination/detection device. Alternatively a series of tests can be measured electrochemically and reported. Only those tests, which are required at the time, the sample is taken need to be reported, though all tests are carried out.

Abstract: A system for identification of animals. The system includes an animal identification device adapted for application to an animal and a device for secure storage of organic material taken from the animal to be identified by the identification device. The storage device and identification device each are marked with a common identifier. The identification device and the storage device are mounted, prior to use, in a holder which can be in the form of a moulded tray.

Abstract: A diagnostic device for performing a diagnostic blood test of a subject comprising a thimble-like element adapted to be engaged with the subject's finger, a puncturing unit for producing a blood sample from the subject's finger, and an at least one test element in flow communication with said blood sample.

Abstract: A blood testing apparatus includes a device for withdrawing blood, a membrane-type testing element, an evaluating device, and a display device forming a complete system which can be manipulated as a single piece of apparatus. Multiple testing elements can be inserted into the apparatus and brought successively to a work position for carrying out several measurements. The blood withdrawing device includes multiple pricking elements. One pricking element is pushed through one testing element and pricks the surface of the skin of a user. The pricking position is disposed so that blood withdrawn from the surface of the skin can impinge upon the testing element.

Abstract: Body fluid testing device for analyzing a body fluid comprises a test media tape adapted to collect the body fluid. The test media tape comprises a tape and test media portions. A free tape portion without test medium is located between successive test media portions. The testing device further comprises a supply portion. The supply portion comprises a housing in which uncontaminated test media tape is contained. The housing further has an opening for withdrawing test media tape from the housing. The testing device further has a sealing means for closing the opening against the surrounding. A free tape portion of the test media tape is located between a wall of the housing and the sealing means when the sealing means closes the opening. Further aspects concern a test media cassette with sealing means and a method for providing test media while holding them sealed against humidity during onboard storage.

Abstract: A portable medical analyzer comprising a sampling module with a sample port for receiving body fluid, an assay sensor module for analysis of the body fluid, an analytical detector module with detection of information from the assay, and a communications module for transferring the information to a remote location via a wired or wireless network.

Abstract: An integrated device is for sampling and testing an analyte. The device generally includes a housing, a lancing device for sampling an analyte, a test strip for substantially capturing at least a portion of the analyte, and a display unit for displaying a result corresponding to the captured portion of the analyte. A method includes performing a single operation to sample an analyte, to capture the sampled analyte, to perform testing on the sampled analyte, and to display a result corresponding to the performed test. A method includes using an integrated sampling and testing device placing the device the device on a test site of a subject, such as a patient, and performing the single operation to obtain a test result. The sampling and testing of analytes may involve testing analytes in blood, such as the blood of a diabetic patient.

Abstract: The invention concerns a sensor cassette that can be inserted into an analyzer comprising a continuous measuring channel for receiving fluidic media and sensory elements for determining chemical and/or physical parameters of the fluidic media. According to the invention the sensor cassette consists of at least two permanently connected but separately manufactured modules which each have a housing and a measuring channel section wherein the measuring channel sections of adjacent modules are connected to the continuous measuring channel by a fluidic coupling and wherein at least one of the connected modules is designed as a sensor module and has a sensor array comprising at least two sensory elements. Furthermore, a memory element is allocated to the sensor cassette on which specific information for the sensor cassette in particular with regard to its construction from the respective modules is stored.

Abstract: A diagnostic agent is delivered intravaginally or to the interlabial space by positioning an interlabial device, such as an absorbent pad, between the labia. The pad is retained between the labia to deliver an active agent, or allow a reaction with a diagnostic agent. Alternatively, the pad is applied after the diagnostic agent is administered, to help reduce discomfort to the subject, or loss of the diagnostic agent. The active agent may be carried by the pad itself, or in an intravaginal extension of the pad, or separately in a suppository or other dosage form. In particular examples, the pad has a smaller minor portion superimposed on a larger major portion, and the smaller minor portion is inserted as a leading edge between the labia of the subject to facilitate interlabial insertion. In another example, the pad is placed interlabially after insertion of an agent.

Abstract: A device and method are provided to monitor for early detection of anomalous conditions in a discharge fluid through a catheter tube. A liquid sensor is configured to detect the presence of liquid in the catheter tube. A unique photo-Darlington turbidity sensor may be configured to monitor turbidity of a discharge liquid exiting through the catheter tube. A color sensor may be configured to monitor color of the discharge liquid exiting through the catheter tube. A processing circuit may be coupled to the liquid sensor, photo-Darlington turbidity sensor, and color sensor and configured to determine whether an anomalous condition exists based on readings provided by the liquid sensor, photo-Darlington turbidity sensor, and/or color sensor. A warning device provides an alert if an anomalous condition is detected.

Abstract: A body fluid sampling system for use on a tissue site includes a single drive force generator. A plurality of penetrating members are operatively coupled to the force generator. The force generator moves each of the members along a path out of a housing with a penetrating member exit, into the tissue site, stops in the tissue site, and withdraws out of the tissue site. A flexible support member couples the penetrating members to define a linear array. The support member is movable and configured to move each of the penetrating members to a launch position associated with the force generator.

Abstract: A sensor and a lancet are integrated with each other. A thin strip-shaped sensor and a lancet are integrated so that the lancet moves in parallel, along a longitudinal direction of the sensor. A measuring device to which an integrated lancet and sensor is attached is provided with a function of driving the attached lancet.

Abstract: A sensor array designed to be continuously indexed through a compatible blood glucose test monitor for the purpose of conducting multiple consecutive blood glucose measurements. The sensor array can be configured to substantially conform to a non-planar surface. In one embodiment, the sensor array includes first and second test sensors which are hingedly coupled together through a pin and socket interconnection. In another embodiment, the sensor array includes a unitary, non-conductive substrate which is scored to define one or more fold lines, a first set electrodes deposited on the substrate to define a first test sensor, and a second set of electrodes deposited on the substrate to define a second test sensor.

Abstract: Apparatus for quick screening for vaginal moisture pH level as related to a pre-selected pH level, comprising a manipulable element including a probe insertible into the vagina, at least one pH indicator on the element, the indicator characterized as producing a color which corresponds to pH level of vaginal moisture contacting the indicator, and a local comparison zone on the element having a color corresponding to a predetermined pH level, and positioned and shaped for quick color comparison with the color of the indicator after indicator contact with vaginal moisture. A test site for vaginosis may also be located on the probe, in non-interfering relation with said indicator and/or said zone.